嗜铬细胞瘤患者的炎症评分。

IF 5 2区 医学 Q1 ENDOCRINOLOGY & METABOLISM Journal of Clinical Endocrinology & Metabolism Pub Date : 2025-02-18 DOI:10.1210/clinem/dgae284
Chiara Parazzoli, Alessandro Prete, Vittoria Favero, Carmen Aresta, Valentina Pucino, John Ayuk, Miriam Asia, Yasir S Elhassan, Iacopo Chiodini, Cristina L Ronchi
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引用次数: 0

摘要

背景:嗜铬细胞瘤与全身炎症有关,但其潜在机制尚不清楚。因此,我们研究了嗜铬细胞瘤患者血浆甲肾上腺素水平与血液学指标(作为炎症的替代指标)之间的关系,以及术前α-受体阻滞治疗的影响:我们回顾性研究了68名接受肾上腺切除术的嗜铬细胞瘤患者(中位年龄53岁,64.7%为女性)和两组年龄、性别和体重指数(BMI)相匹配的对照组:68名无功能肾上腺皮质肿瘤(NFAT)患者和53名原发性高血压(EAH)患者。全血细胞计数(CBC)和几项基于炎症的评分[中性粒细胞与淋巴细胞比值(NLR)、血小板与淋巴细胞比值(PLR)、淋巴细胞与单核细胞比值(LMR)、系统免疫炎症指数(SII)、预后营养指数(PSR)、免疫系统炎症指数(SII)]、在肾上腺切除术后(26 例)和术前α-受体阻滞治疗前后(29 例)对所有患者进行了评估,并对嗜铬细胞瘤亚组进行了评估。结果显示与 NFAT 和 EAH 相比,嗜铬细胞瘤患者的炎症状态更高,CBC 和炎症评分均显示了这一点。血浆甲肾上腺素水平与 NLR(r=0.4631)、PLR(r=0.3174)、SII(r=0.3709)呈正相关,而与 LMR(r=0.4368)和 PNI(r=0.3741)呈负相关,即使在调整年龄、性别、种族、体重指数和肿瘤大小(PLR 除外)后也是如此。肾上腺切除术后,我们观察到 NLR(p=0.001)、PLR(p=0.003)、SII(p=0.004)降低,同时 LMR(p=0.0002)升高。同样,α-受体阻滞治疗可降低NLR(p=0.007)和SII(p=0.03):结论:嗜铬细胞瘤患者基于炎症的评分显示了与血浆肾上腺素水平相关的促炎症变化,肾上腺切除术和α-受体阻滞剂可改善这种变化。
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Inflammation-based Scores in Patients With Pheochromocytoma.

Background: Pheochromocytoma is associated with systemic inflammation but the underlying mechanisms are unclear. Therefore, we investigated the relationship between plasma metanephrine levels and hematological parameters-as a surrogate of inflammation-in patients with pheochromocytoma and the influence of preoperative α-blockade treatment.

Design and methods: We retrospectively studied 68 patients with pheochromocytoma who underwent adrenalectomy (median age, 53 years; 64.7% females) and 2 control groups matched for age, sex, and body mass index: 68 patients with nonfunctioning adrenocortical tumors and 53 with essential hypertension. The complete blood count and several inflammation-based scores (neutrophil-to-lymphocyte ratio [NLR], platelet-to-lymphocyte ratio [PLR], lymphocyte-to-monocyte ratio [LMR], systemic-immune-inflammation index [SII], prognostic-nutrition index) were assessed in all patients and, in a subset of pheochromocytomas, after adrenalectomy (n = 26) and before and after preoperative α-blockade treatment (n = 29).

Results: A higher inflammatory state, as indicated by both complete blood count and inflammation-based scores, was observed in patients with pheochromocytoma compared with nonfunctioning adrenocortical tumors and essential hypertension. Plasma metanephrine levels showed a positive correlation with NLR (r = 0.4631), PLR (r = 0.3174), and SII (r = 0.3709) and a negative correlation with LMR (r = 0.4368) and prognostic-nutrition index (r = 0.3741), even after adjustment for age, sex, ethnicity, body mass index, and tumor size (except for PLR). After adrenalectomy, we observed a reduction in NLR (P = .001), PLR (P = .003), and SII (P = .004) and a concomitant increase in LMR (P = .0002). Similarly, α-blockade treatment led to a reduction in NLR (P = .007) and SII (P = .03).

Conclusion: Inflammation-based scores in patients with pheochromocytoma showed pro-inflammatory changes that correlated with plasma metanephrine levels and are ameliorated by adrenalectomy and α-blockade.

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来源期刊
Journal of Clinical Endocrinology & Metabolism
Journal of Clinical Endocrinology & Metabolism 医学-内分泌学与代谢
CiteScore
11.40
自引率
5.20%
发文量
673
审稿时长
1 months
期刊介绍: The Journal of Clinical Endocrinology & Metabolism is the world"s leading peer-reviewed journal for endocrine clinical research and cutting edge clinical practice reviews. Each issue provides the latest in-depth coverage of new developments enhancing our understanding, diagnosis and treatment of endocrine and metabolic disorders. Regular features of special interest to endocrine consultants include clinical trials, clinical reviews, clinical practice guidelines, case seminars, and controversies in clinical endocrinology, as well as original reports of the most important advances in patient-oriented endocrine and metabolic research. According to the latest Thomson Reuters Journal Citation Report, JCE&M articles were cited 64,185 times in 2008.
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